Product NDC: | 76344-4001 |
Proprietary Name: | Laser Sun Block 100 SPF50 |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE |
Active Ingredient(s): | 7.5; 5; 2.49; 4.8 g/100mL; g/100mL; g/100mL; g/100mL & nbsp; OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76344-4001 |
Labeler Name: | Humex,Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130515 |
Package NDC: | 76344-4001-2 |
Package Description: | 1 TUBE in 1 BOX (76344-4001-2) > 50 mL in 1 TUBE (76344-4001-1) |
NDC Code | 76344-4001-2 |
Proprietary Name | Laser Sun Block 100 SPF50 |
Package Description | 1 TUBE in 1 BOX (76344-4001-2) > 50 mL in 1 TUBE (76344-4001-1) |
Product NDC | 76344-4001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130515 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Humex,Inc. |
Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 7.5; 5; 2.49; 4.8 |
Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL |
Pharmaceutical Classes |